WO2004087575A1 - Mg2mm’ 06+x, ( m=y, rare earth metal, and m’=sn, sb, zr, hf, and ta) compounds and a method for the production of the same - Google Patents
Mg2mm’ 06+x, ( m=y, rare earth metal, and m’=sn, sb, zr, hf, and ta) compounds and a method for the production of the same Download PDFInfo
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Definitions
- This invention relates to a new group of complex ceramic oxides
- the complex ceramic powders of the present invention are
- microwave dielectrics and as co-fired microwave components for electrodes of Fuel cells, as catalyst (solid photocatalysts, oxidation catalysts), as gas monitoring
- magnesium bearing ceramic oxides reported for possible use in electronic ceramic applications are Sr 2 MgMoO 6 , La 2 MgTiO 6 , Gd 2 MgTiO 6 , Gd 2 MgZrO 6 and La 2 MgGeO 6 , (C D Bradle and V J Fratello, preparation of perovskite oxides for high Tc superconductor substrates; journal of Materials Research, volume-5, Number-10, pages-2160-2164 year 1990;). Most of the above mentioned compounds had a perovskite structure.
- Pyrochlore structures are the structures with the general formula A 2 B 2 O 7 , where A atoms are 8 coordinated ad B atoms are 6 coordinated with one extra O-atom.
- a atoms are 8 coordinated ad B atoms are 6 coordinated with one extra O-atom.
- many pyrochlore compounds with more complicated composition (AA') 2 (BB) 2 O 7 have been synthesized.
- AA' AA'
- BB BB 2 O 7
- the ratio of the ionic radius of the cation at the A site to that at the B site must be between 1.46 and 1.80 and (2) the chemical valencies of the various ions must made the compound neutral.
- pyrochlore compounds exhibit high Ionic conductivity and can be used as electrodes for Fuel cells, egs, Gd 2 TiMoO 7+x ; Gd 2 TiO 7+x (P Holtappels, F W Poulsen and M Mogensen; Electrical conductivities and chemical stabilities of mixed conducting pyrochlores for Solid oxide fuel cell applications; Solid State Ionics, vol. 135, pp 675-679 (2000)).
- Pyrochlore oxides also exhibit catalytic properties and are used as solid photocatalysts (eg.
- Pyrochlores have been used in active and passive electronic applications. They are recently recognized as potential candidates for temperature stable, low loss, high permitivity dielectric applications and in temperature stable and temperature compensating dielectrics; microwave dielectrics and as co-fired microwave components (P Holtappels, F W Poulsen and M Mogensen; Electrical conductivities and chemical stabilities of mixed conducting pyrochlores for SOFC applications,; Solid State Ionics, vol. 135, pp 675-679 (2000)).
- the main objectives of the present invention is to provide a novel Magnesium based class of complex ceramic oxides, that could be used (i) for active and passive electronic applications, (ii) for temperature stable, low loss, high permitivity dielectric applications (iii) for temperature stable and temperature compensating dielectrics; microwave dielectrics and as co-fired microwave components (iv) for electrodes for Fuel cells (v) as catalyst (solid photocatalysts, oxidation catalysts) (vi) as gas monitoring sensors, (vii) as possible host for radioactive wastes, and (viii) as host for fluorescence centers.
- Yet another objective of the present invention is to provide a method for the preparation of a novel magnesium bearing class of complex ceramic oxides having the above formula, structure and uses.
- the compounds employed in step (i) may be selected from their oxides, carbonates, chlorides, alkoxides, nitrates, sulphates etc; preferably the salts used are selected from oxides or carbonates.
- the mixture obtained in step (i) may be ball milled or mixed with wetting medium.
- the wetting medium may be water, alcohol, acetone or any other organic solvent.
- the resultant ball milled slurry may be dried to remove the liquid and obtain dry powder.
- the complex ceramic powders of the present invention are useful as the complex ceramic powders of the present invention.
- step (ii) the mixture obtained in step (i) is ball milled or mixed with a wetting medium
- the resultant ball milled slurry obtained is dried to remove the liquid and obtain dry powder.
- Heating the resultant mixture to a temperature in the range 1000- 1600°C as required for different duration ranging from 3 hour to 50 hours, either in a single step or by taking out the reactant after few hours of heating, checking for phase formation and heating it again after grinding if necessary, upto a maximum of 5 intermediate grindings may be required.
- the compounds employed in the process are selected from their oxides, carbonates chlorides, alkoxides, nitrates, sulfates etc. and preferably the salts used are selected from oxides or carbonate.
- the wetting medium used in the process is selected from water, alcohol, acetone or any other organic solvent.
- novel compound obtained is of the formula Mg 2 SmTaO 6 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 NdTaO 6 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 DyTaO 6 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 PrTaO 6 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 GdTaO 6 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is for the formula Mg 2 EuTaO 6 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 LaTaO 6 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 DySbO 6 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 SmZrO 5 5 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 NdZrO 5 . 5 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 DyZrO 5 5 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 LaSnO 5 5 as nanoparticle having pyrochlore structure wherein minor variation in the composition upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 GdZrO 5 5 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 EuZrO 5 5 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 LaZrO 5 5 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- novel compound obtained is of the formula Mg 2 PrZrO 5 5 as nanoparticle having pyrochlore structure wherein minor variation in the compositions upto 8% in any of the metal ions is tolerated for the formation of the phase.
- Example-1 Magnesium Samarium Tantalate (Mg 2 SmTaQ 6 ), Magnesium Samarium Tantalate (Mg 2 SmTaO 6 ), for example, is obtained by:
- Example-2 Magnesium Lanthanum Stanate (Mg 2 LaSn0 5 . 5 ), Magnesium Lanthanum Stanate (Mg 2 LaSnO 5 5 ), for example, is obtained by;
- Example-3 Magnesium Dysprosium Antimonate (Mg 2 DySb0 6 ),
- Magnesium Dysprosium Antimonate (Mg 2 DySbO 6 ), for example, is obtained by;
- Example-4 Magnesium Neodymium Zirconate (Mg2NdZrO6),
- Magnesium Neodymium Zirconate (Mg2NdZrO6), for example, is obtained by; (i) taking four gram molecular weight of Magnesium Carbonate (MgCO 3 ), one gram molecular weight of Neodymium oxide (Nd 2 O 3 ), and one gram molecular weight of Zirconium oxide (ZrO 2 ).
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Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2003262231A AU2003262231A1 (en) | 2003-03-31 | 2003-03-31 | Mg2mm' 06+x, ( m=y, rare earth metal, and m'=sn, sb, zr, hf, and ta) compounds and a method for the production of the same |
DE60307905T DE60307905T2 (de) | 2003-03-31 | 2003-03-31 | Mg2mm' 06+x, ( m=y, seltenes erdmetall und m'=sn, sb, zr, hf und ta)-verbindungen und zugehöriges herstellungsverfahren |
CNB038262568A CN100348497C (zh) | 2003-03-31 | 2003-03-31 | MG2MM'O6+x(M=Y,稀土金属;M'=SN,SB,ZR,HF和TA)化合物及其制备方法 |
JP2004570100A JP4575171B2 (ja) | 2003-03-31 | 2003-03-31 | Mg2MM’O6+x、(M=Y、希土類金属、およびM’=SN、SB、ZR、HF、およびTA)化合物、およびその製造方法 |
PCT/IN2003/000131 WO2004087575A1 (en) | 2003-03-31 | 2003-03-31 | Mg2mm’ 06+x, ( m=y, rare earth metal, and m’=sn, sb, zr, hf, and ta) compounds and a method for the production of the same |
CA2520555A CA2520555C (en) | 2003-03-31 | 2003-03-31 | Mg2mm' 06+x, ( m=y, rare earth metal, and m'=sn, sb, zr, hf, and ta) compounds and a method for the production of the same |
EP03816531A EP1608595B1 (en) | 2003-03-31 | 2003-03-31 | Mg2mm' 06+x, ( m=y, rare earth metal, and m'=sn, sb, zr, hf, and ta) compounds and a method for the production of the same |
Applications Claiming Priority (1)
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PCT/IN2003/000131 WO2004087575A1 (en) | 2003-03-31 | 2003-03-31 | Mg2mm’ 06+x, ( m=y, rare earth metal, and m’=sn, sb, zr, hf, and ta) compounds and a method for the production of the same |
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WO2004087575A1 true WO2004087575A1 (en) | 2004-10-14 |
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PCT/IN2003/000131 WO2004087575A1 (en) | 2003-03-31 | 2003-03-31 | Mg2mm’ 06+x, ( m=y, rare earth metal, and m’=sn, sb, zr, hf, and ta) compounds and a method for the production of the same |
Country Status (7)
Country | Link |
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EP (1) | EP1608595B1 (zh) |
JP (1) | JP4575171B2 (zh) |
CN (1) | CN100348497C (zh) |
AU (1) | AU2003262231A1 (zh) |
CA (1) | CA2520555C (zh) |
DE (1) | DE60307905T2 (zh) |
WO (1) | WO2004087575A1 (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102942928A (zh) * | 2012-11-30 | 2013-02-27 | 苏州大学 | 一种锆酸盐基红色荧光粉、制备方法及应用 |
WO2016185042A1 (de) * | 2015-05-20 | 2016-11-24 | H1 Energy B.V. | Photokatalysator |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2012105583A1 (en) * | 2011-01-31 | 2012-08-09 | Canon Kabushiki Kaisha | Composition for optical members and optical member |
WO2012105584A1 (en) * | 2011-01-31 | 2012-08-09 | Canon Kabushiki Kaisha | Composition for optical members and optical member |
CN102191048B (zh) * | 2011-03-18 | 2013-08-14 | 中国科学院上海光学精密机械研究所 | 铕激活的发光二极管用红色荧光粉及其制备方法 |
WO2015004529A2 (en) * | 2013-07-11 | 2015-01-15 | Sabic Global Technologies B.V. | Method of making pyrochlores |
CN107986785B (zh) * | 2017-12-09 | 2020-11-24 | 桂林理工大学 | 高品质因数微波介电陶瓷材料及其制备方法 |
CN111410514B (zh) * | 2020-03-31 | 2021-01-05 | 青海大学 | 一种光学测温材料及其制备方法和非接触式测温材料 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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US20020110517A1 (en) * | 2000-03-28 | 2002-08-15 | Council Of Scientific And Industrial Research | Single step process for the synthesis of nanoparticles of ceramic oxide powders |
Family Cites Families (6)
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JPH04175223A (ja) * | 1990-11-06 | 1992-06-23 | Sumitomo Metal Mining Co Ltd | 多成分系複合ペロブスカイト固溶体の製造方法 |
JPH05254841A (ja) * | 1992-03-12 | 1993-10-05 | Sumitomo Sitix Corp | 酸化物粉末の製造方法 |
JP3401834B2 (ja) * | 1993-04-27 | 2003-04-28 | ソニー株式会社 | 誘電体材料 |
JPH0733441A (ja) * | 1993-07-26 | 1995-02-03 | Nippon Steel Corp | 複合酸化物の製造方法 |
CN1089249A (zh) * | 1993-11-15 | 1994-07-13 | 天津大学 | 抗高温老化及高韧性psz陶瓷 |
JP2001073142A (ja) * | 1999-09-02 | 2001-03-21 | Internatl Superconductivity Technology Center | 複合ペロブスカイト酸化物(例えばa3+2b+b5+o6,a2+2b3+b5+o6,a2+3b2+b5+2o9等)の薄膜の原料とその成長法 |
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2003
- 2003-03-31 JP JP2004570100A patent/JP4575171B2/ja not_active Expired - Fee Related
- 2003-03-31 CA CA2520555A patent/CA2520555C/en not_active Expired - Fee Related
- 2003-03-31 EP EP03816531A patent/EP1608595B1/en not_active Expired - Fee Related
- 2003-03-31 AU AU2003262231A patent/AU2003262231A1/en not_active Abandoned
- 2003-03-31 WO PCT/IN2003/000131 patent/WO2004087575A1/en active IP Right Grant
- 2003-03-31 DE DE60307905T patent/DE60307905T2/de not_active Expired - Lifetime
- 2003-03-31 CN CNB038262568A patent/CN100348497C/zh not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020110517A1 (en) * | 2000-03-28 | 2002-08-15 | Council Of Scientific And Industrial Research | Single step process for the synthesis of nanoparticles of ceramic oxide powders |
Non-Patent Citations (3)
Title |
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ASHA M. JOHN ET AL.: "Synthesis and rapid densification of nanoparticles of barium praseodymium hafnium oxide: a new complex perovskite", JOURNAL OF NANOPARTICLE RESEARCH, vol. 3, 2001, pages 413 - 417, XP009025406 * |
J. KOSHY ET AL.: "Rare Earth Barium Stannates: Synthesis, Characterization, and Potential Use as Substrates for YBa2Cu3O7-delta Superconductor", J. AM. CERAM. SOC., vol. 78, no. 11, 1995, pages 3088 - 3092, XP001179275 * |
WARIAR P R S ET AL: "Development of superconducting YBa2Cu3O7 - delta and YBa2Cu3O7 - delta-Ag thick film by dip coating on SmBa2SbO6, a new ceramic substrate material", APPLIED SUPERCONDUCTIVITY, PERGAMON PRESS, EXETER, GB, vol. 4, no. 1, 1996, pages 111 - 117, XP004008880, ISSN: 0964-1807 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102942928A (zh) * | 2012-11-30 | 2013-02-27 | 苏州大学 | 一种锆酸盐基红色荧光粉、制备方法及应用 |
WO2016185042A1 (de) * | 2015-05-20 | 2016-11-24 | H1 Energy B.V. | Photokatalysator |
Also Published As
Publication number | Publication date |
---|---|
CA2520555C (en) | 2012-01-03 |
JP4575171B2 (ja) | 2010-11-04 |
CN1759067A (zh) | 2006-04-12 |
DE60307905T2 (de) | 2007-10-11 |
CN100348497C (zh) | 2007-11-14 |
JP2006514911A (ja) | 2006-05-18 |
DE60307905D1 (de) | 2006-10-05 |
CA2520555A1 (en) | 2004-10-14 |
EP1608595A1 (en) | 2005-12-28 |
AU2003262231A1 (en) | 2004-10-25 |
EP1608595B1 (en) | 2006-08-23 |
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